N-(1,2,3,4-Tetrahydro-2-methyl-4-phenyl-8-isoquinolyl)-4-morpholineacetamide maleate

Base Information

Chemical Name:N-(1,2,3,4-Tetrahydro-2-methyl-4-phenyl-8-isoquinolyl)-4-morpholineacetamide maleate
CAS No.:91454-33-0
Molecular Formula:2C₄H₄O₄*C₂₂H₂₇N₃O₂
Molecular Weight:597.622
Hs Code.:

Synonyms:N-(1,2,3,4-Tetrahydro-2-methyl-4-phenyl-8-isoquinolyl)-4-morpholineacetamide maleate;91454-33-0;4-Morpholineacetamide, N-(1,2,3,4-tetrahydro-2-methyl-4-phenyl-8-isoquinolyl)-, (Z)-2-butenedioate (1:2);SCHEMBL11013519

Suppliers and Price of N-(1,2,3,4-Tetrahydro-2-methyl-4-phenyl-8-isoquinolyl)-4-morpholineacetamide maleate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of N-(1,2,3,4-Tetrahydro-2-methyl-4-phenyl-8-isoquinolyl)-4-morpholineacetamide maleate

Chemical Property:

Hydrogen Bond Donor Count:5
Hydrogen Bond Acceptor Count:12
Rotatable Bond Count:8
Exact Mass:597.23224432
Heavy Atom Count:43
Complexity:607

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN1CC(C2=C(C1)C(=CC=C2)NC(=O)CN3CCOCC3)C4=CC=CC=C4.C(=CC(=O)O)C(=O)O.C(=CC(=O)O)C(=O)O
Isomeric SMILES:CN1CC2=C(C(C1)C3=CC=CC=C3)C=CC=C2NC(=O)CN4CCOCC4.C(=C\C(=O)O)\C(=O)O.C(=C\C(=O)O)\C(=O)O

Technology Process of N-(1,2,3,4-Tetrahydro-2-methyl-4-phenyl-8-isoquinolyl)-4-morpholineacetamide maleate

There total 3 articles about N-(1,2,3,4-Tetrahydro-2-methyl-4-phenyl-8-isoquinolyl)-4-morpholineacetamide maleate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 24526-64-5
nomifensine

: 91454-33-0,99633-77-9
N-(2-Methyl-4-phenyl-1,2,3,4-tetrahydro-isoquinolin-8-yl)-2-morpholin-4-yl-acetamide; compound with (Z)-but-2-enedioic acid

Guidance literature:: Multi-step reaction with 3 steps

1: 87 percent / K₂CO₃ / acetone / 0.5 h / Heating

2: benzene / Heating

3: ethanol

With potassium carbonate; In ethanol; acetone; benzene;